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| | 6-Chloro-1H-pyrazolo[3,4-d]pyrimidine Basic information |
| | 6-Chloro-1H-pyrazolo[3,4-d]pyrimidine Chemical Properties |
| Melting point | >100°C (dec.) | | Boiling point | 287.9±23.0 °C(Predicted) | | density | 1.84±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | solubility | DMSO (Slightly), Ethyl Acetate (Slightly) | | form | Solid | | pka | 9.27±0.20(Predicted) | | color | Pale Yellow | | Stability: | Moisture Sensitive | | InChI | InChI=1S/C5H3ClN4/c6-5-7-1-3-2-8-10-4(3)9-5/h1-2H,(H,7,8,9,10) | | InChIKey | CZAPPYRAFCOFOL-UHFFFAOYSA-N | | SMILES | C1(Cl)=NC=C2C=NNC2=N1 |
| | 6-Chloro-1H-pyrazolo[3,4-d]pyrimidine Usage And Synthesis |
| Uses | Pyrazolo[3,4-d]pyrimidines have a close structural resemblance to the substrates for the enzyme xanthine oxidase, hypoxanthine (6-hydroxypurine) and xanthine (2,6-dihydroxypurine). These compounds are capable of binding to the enzyme and strongly inhibit its activity. They have been studied for their role in the treatment and prophylaxis of hyperuricemia in human patients as well as potential anti-tumor agents. | | Synthesis | To a stirred solution of hydrazine in THF, 2,4-Dichloro-pyrimidine-5-carbaldehyde was added and the mixture was stirred at room temperature for 30 min. The mixture was poured into water and extracted with EtOAc. The extract was dried with sodium sulfate and the solvent was removed to give an orange solid. Yield_82%
![6-Chloro-1H-pyrazolo[3,4-d]pyrimidine](/NewsImg/2023-11-06/6383488556496658508963214.jpg "6-Chloro-1H-pyrazolo[3,4-d]pyrimidine")
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| | 6-Chloro-1H-pyrazolo[3,4-d]pyrimidine Preparation Products And Raw materials |
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